(R)-3-((tert-Butoxycarbonyl)amino)-3-(m-tolyl)propanoic acid

95%

Reagent Code: #231435
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CAS Number 464930-76-5

science Other reagents with same CAS 464930-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.33 g/mol
Formula C₁₅H₂₁NO₄
badge Registry Numbers
MDL Number MFCD03427934
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for constructing complex organic molecules with high enantioselectivity. Commonly employed in peptide mimetics and drug discovery research where controlled stereochemistry is critical for biological activity. The Boc-protected amine and carboxylic acid allow for selective coupling reactions, enabling stepwise assembly of larger molecular structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿510.00
inventory 250mg
10-20 days ฿1,220.00
(R)-3-((tert-Butoxycarbonyl)amino)-3-(m-tolyl)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for constructing complex organic molecules with high enantioselectivity. Commonly employed in peptide mimetics and drug discovery research where controlled stereochemistry is critical for biological activity. The Boc-protected amine and carboxylic acid allow for selective coupling

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for constructing complex organic molecules with high enantioselectivity. Commonly employed in peptide mimetics and drug discovery research where controlled stereochemistry is critical for biological activity. The Boc-protected amine and carboxylic acid allow for selective coupling reactions, enabling stepwise assembly of larger molecular structures.

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